Canonical Allele Identifier: CA1979406135
Gene: OVOL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65791886_65791896delinsCCACTCAGCGA , CM000673.2:g.65791886_65791896delinsCCACTCAGCGA GRCh38
NC_000011.9:g.65559357_65559367delinsCCACTCAGCGA , CM000673.1:g.65559357_65559367delinsCCACTCAGCGA GRCh37
NC_000011.8:g.65315933_65315943delinsCCACTCAGCGA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000335987.8:c.101-2145_101-2135delinsCCACTCAGCGA MANE Select ENSP00000337862.3:n.101-2145_101-2135delinsCCACTCAGCGA
ENST00000335987.7:c.101-2145_101-2135delinsCCACTCAGCGA ENSP00000337862.3:n.101-2145_101-2135delinsCCACTCAGCGA
ENST00000531907.1:n.361-432_361-422delinsCCACTCAGCGA
NM_004561.3:c.101-2145_101-2135delinsCCACTCAGCGA NP_004552.2:n.101-2145_101-2135delinsCCACTCAGCGA
XM_005274018.3:c.-86-2145_-86-2135delinsCCACTCAGCGA XP_005274075.1:n.-86-2145_-86-2135delinsCCACTCAGCGA
XM_011545067.1:c.-86-2145_-86-2135delinsCCACTCAGCGA XP_011543369.1:n.-86-2145_-86-2135delinsCCACTCAGCGA
XM_011545068.1:c.-87+1023_-87+1033delinsCCACTCAGCGA XP_011543370.1:n.-87+1023_-87+1033delinsCCACTCAGCGA
XM_011545067.2:c.-86-2145_-86-2135delinsCCACTCAGCGA XP_011543369.1:n.-86-2145_-86-2135delinsCCACTCAGCGA
XM_011545068.3:c.-87+1023_-87+1033delinsCCACTCAGCGA XP_011543370.1:n.-87+1023_-87+1033delinsCCACTCAGCGA
XM_017017837.1:c.-86-2145_-86-2135delinsCCACTCAGCGA XP_016873326.1:n.-86-2145_-86-2135delinsCCACTCAGCGA
NM_004561.4:c.101-2145_101-2135delinsCCACTCAGCGA MANE Select NP_004552.2:n.101-2145_101-2135delinsCCACTCAGCGA